Quality Systems Co-op
Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.
We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.
We are seeking a motivated and detail-oriented student to join our Quality Systems team for a 6–9 month placement. This role offers hands-on experience in a dynamic manufacturing environment, supporting compliance with regulatory standards and continuous improvement initiatives.
Key Responsibilities:
- Assist in maintaining and improving the Quality Management System (QMS) in compliance with ISO 13485, FDA, and other applicable regulations.
- Support document control activities, including review, approval, and archiving of quality documentation.
- Participate in internal audits and help prepare for external audits and inspections.
- Assist with change control processes and ensure timely updates to quality records.
- Collaborate with cross-functional teams to support CAPA (Corrective and Preventive Actions) and NCR (Non-Conformance Reports) processes.
- Contribute to data analysis and reporting for quality metrics and KPIs.
- Support training initiatives related to quality systems and compliance.
Requirements:
- Currently enrolled in a degree program in Quality, Engineering, Science, or related discipline.
- Strong attention to detail and organizational skills.
- Excellent communication skills and ability to work in a team environment.
- Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
- Interest in quality systems and regulatory compliance within a medical device or healthcare setting.
What We Offer:
- Practical experience in a regulated manufacturing environment.
- Exposure to quality systems and compliance processes.
- Mentorship and guidance from experienced professionals.
- Opportunity to develop skills that support a career in Quality Assurance or Regulatory Affairs.
Reasonable Accommodation
Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link
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Address
- FIELD SERVICE SPECIALIST Atlanta, Georgia
- Field Service Technician – Atlanta, GA Atlanta, Georgia
- Therapiespezialist - Acute Therapies (w/m/d) Austria